Dou Lingling, Jia Xiaoyun, Wei Hengling, Fan Shuli, Wang Hantao, Guo Yaning, Duan Shan, Pang Chaoyou, Yu Shuxun
State Key Laboratory of Cotton Biology, Institute of Cotton Research of CAAS, Anyang, Henan, P. R. China.
Weinan Institute of Agricultural Sciences, Weinan, Shaanxi, P. R. China.
PLoS One. 2017 Jul 17;12(7):e0179141. doi: 10.1371/journal.pone.0179141. eCollection 2017.
DNA methylation is an important epigenetic modification regulating gene expression, genomic imprinting, transposon silencing and chromatin structure in plants and plays an important role in leaf senescence. However, the DNA methylation pattern during Gossypium hirsutum L. cotyledon senescence is poorly understood. In this study, global DNA methylation patterns were compared between two cotyledon development stages, young (J1) and senescence (J2), using methylated DNA immunoprecipitation (MeDIP-Seq). Methylated cytosine occurred mostly in repeat elements, especially LTR/Gypsy in both J1 and J2. When comparing J1 against J2, there were 1222 down-methylated genes and 623 up-methylated genes. Methylated genes were significantly enriched in carbohydrate metabolism, biosynthesis of other secondary metabolites and amino acid metabolism pathways. The global DNA methylation level decreased from J1 to J2, especially in gene promoters, transcriptional termination regions and regions around CpG islands. We further investigated the expression patterns of 9 DNA methyltransferase-associated genes and 2 DNA demethyltransferase-associated genes from young to senescent cotyledons, which were down-regulated during cotyledon development. In this paper, we first reported that senescent cotton cotyledons exhibited lower DNA methylation levels, primarily due to decreased DNA methyltransferase activity and which also play important role in regulating secondary metabolite process.
DNA甲基化是一种重要的表观遗传修饰,可调节植物中的基因表达、基因组印记、转座子沉默和染色质结构,并在叶片衰老中发挥重要作用。然而,人们对陆地棉子叶衰老过程中的DNA甲基化模式了解甚少。在本研究中,利用甲基化DNA免疫沉淀技术(MeDIP-Seq)比较了两个子叶发育阶段,即幼嫩期(J1)和衰老期(J2)的全基因组DNA甲基化模式。甲基化胞嘧啶大多出现在重复元件中,尤其是在J1和J2中的LTR/Gypsy元件。比较J1和J2时,有1222个基因发生了甲基化水平下调,623个基因发生了甲基化水平上调。甲基化基因在碳水化合物代谢、其他次生代谢物的生物合成和氨基酸代谢途径中显著富集。全基因组DNA甲基化水平从J1到J2降低,尤其是在基因启动子、转录终止区域和CpG岛周围区域。我们进一步研究了9个DNA甲基转移酶相关基因和2个DNA去甲基化酶相关基因从幼嫩子叶到衰老子叶的表达模式,这些基因在子叶发育过程中表达下调。在本文中,我们首次报道衰老的棉花子叶表现出较低的DNA甲基化水平,这主要是由于DNA甲基转移酶活性降低,并且其在调节次生代谢过程中也发挥重要作用。